In a recent series of three papers, Belokurov, Evans & Le Du and Evans & Belokurov reanalysed the MACHO collaboration data and gave alternative sets of microlensing events and an alternative optical depth to microlensing towards the Large Magellanic Cloud (LMC). Although these authors examined less than 0.2 per cent of the data, they reported that by using a neural net program they had reliably selected a better (and smaller) set of microlensing candidates. Estimating the optical depth from this smaller set, they claimed that the MACHO collaboration overestimated the optical depth by a significant factor and that the MACHO microlensing experiment is consistent with lensing by known stars in the Milky Way and LMC. As we show below, the analysis by these authors contains several errors, and as a result their conclusions are incorrect. Their efficiency analysis is in error, and since they did not search through the entire MACHO data set, they do not know how many microlensing events their neural net would find in the data nor what optical depth their method would give. Examination of their selected events suggests that their method misses low signal‐to‐noise ratio events and thus would have lower efficiency than the MACHO selection criteria. In addition, their method is likely to give many more false positives (non‐lensing events identified as lensing). Both effects would increase their estimated optical depth. Finally, we note that the EROS discovery that LMC event 23 is a variable star reduces the MACHO collaboration estimates of optical depth and the Macho halo fraction by around 8 per cent, and does open the question of additional contamination.
We present a catalog of 450 high signal-to-noise microlensing events observed by the MACHO collaboration between 1993 and 1999. The events are distributed throughout our fields and, as expected, they show clear concentration toward the Galactic center. No optical depth is given for this sample since no blending efficiency calculation has been performed, and we find evidence for substantial blending. In a companion paper we give optical depths for the sub-sample of events on clump giant source stars, where blending is not a significant effect. Several events with sources that may belong to the Sagittarius dwarf galaxy are identified. For these events even relatively low dispersion spectra could suffice to classify these events as either consistent with Sagittarius membership or as non-Sagittarius sources. Several unusual events, such as microlensing of periodic variable source stars, binary lens events, and an event showing extended source effects are identified. We also identify a number of contaminating background events as cataclysmic variable stars.Comment: 34 pages, 9 figures + 3 example lightcurves, all 564 lightcurves will be available at http://wwwmacho.mcmaster.ca, submitted to ApJ, see companion paper by Popowski et a
We reexamine the usefulness of fitting blended lightcurve models to microlensing photometric data. We find agreement with previous workers (e.g. Wozniak & Paczynski) that this is a difficult proposition because of the degeneracy of blend fraction with other fit parameters. We show that follow-up observations at specific point along the lightcurve (peak region and wings) of high magnification events are the most helpful in removing degeneracies. We also show that very small errors in the baseline magnitude can result in problems in measuring the blend fraction, and study the importance of non-Gaussian errors in the fit results. The biases and skewness in the distribution of the recovered blend fraction is discussed. We also find a new approximation formula relating the blend fraction and the unblended fit parameters to the underlying event duration needed to estimate microlensing optical depth.Comment: 18 pages, 9 figures, submitted to Ap
One leading hypothesis for why we lose our hearing as we age is a decrease in ear metabolism. However, direct measurements of metabolism across a lifespan in any auditory system are lacking. Even if metabolism does decrease with age, a question remains: is a metabolic decrease a cause of age-related auditory decline or simply correlative? We use an insect, the desert locust Schistocerca gregaria, as a physiologically versatile model to understand how cellular metabolism correlates with age and impacts on age-related auditory decline. We found that auditory organ metabolism decreases with age as measured fluorometrically. Next, we measured the individual auditory organ’s metabolic rate and its sound-evoked nerve activity and found no correlation. We found no age-related change in auditory nerve activity, using hook electrode recordings, and in the electrophysiological properties of auditory neurons, using patch-clamp electrophysiology, but transduction channel activity decreased. To further test for a causative role of the metabolic rate in auditory decline, we manipulated metabolism of the auditory organ through diet and cold-rearing but found no difference in sound-evoked nerve activity. We found that although metabolism correlates with age-related auditory decline, it is not causative. Finally, we performed RNA-Seq on the auditory organs of young and old locusts, and whilst we found enrichment for Gene Ontology terms associated with metabolism, we also found enrichment for a number of additional aging GO terms. We hypothesize that age-related hearing loss is dominated by accumulative damage in multiple cell types and multiple processes which outweighs its metabolic decline.
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